Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|December 17, 2008
Gender dysphoria and gender change in an adolescent with 45,X/46,XY mixed gonadal dysgenesisG Ocal, M Berberoğlu, Z Siklar, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 1, 2000
Hajdu-Cheney syndrome with growth hormone deficiency and neuropathyZ Siklar, G Tanyer, Y Dallar, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|December 17, 2008
"Maternal/Neonatal" iodine status in patients with prolonged physiological jaundiceZ Siklar, G Oçal, P Bilir, et al.
Journal of Tropical Pediatrics|March 14, 2001
Multiple dose IVIG treatment in neonatal immune hemolytic jaundiceG Tanyer, Z Siklar, Y Dallar, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|June 5, 2008
Cytokines as a common components of two different disorders: metabolic syndrome and hemophagocytic lymphohystiositosisZ Siklar, M Berberoğlu, Z Uysal, et al.
Acta Endocrinologica (Bucharest, Romania : 2005)|January 23, 2025
THE USE OF ORAL BISPHOSPHONATES IN REFRACTORY SEVERE HYPERCALCEMIA AFTER DENOSUMAB CESSATIONM E Bilici, Z Siklar, E Unal, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 23, 2006
Plasminogen activator inhibitor-1 (PAI-1) gene polymorphism (-675 4G/5G) associated with obesity and vascular risk in childrenM Berberoğlu, O Evliyaoğlu, P Adiyaman, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 3, 2011
Disorders of sexual development: an overview of 18 years experience in the pediatric Endocrinology Department of Ankara UniversityG Ocal, M Berberoğlu, Z Siklar, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 2, 2008
Identification of frequency and distribution of the nine most frequent mutations among patients with 21-hydroxylase deficiency in TurkeyF Sadeghi, N Yurur-Kutlay, M Berberoglu, et al.
Pageof 1